2026 Regulatory Affairs Co-op (6 Months, July 2026 Start)
Haleon
Warren, NJ, USA
Hourly: $24.50; bonus/equity: not specified; benef...
Fda submission documentation review
Electronic data management system maintenance
Full-time on-site work in new jersey
This role supports process improvements and ensures compliance within the electronic data management system for a world-leading consumer healthcare company
Job Summary
This role supports process improvements and ensures compliance within the electronic data management system for a world-leading consumer healthcare company.
The successful candidate will track, categorize, and upload FDA correspondences while maintaining accurate registration metadata for the Haleon portfolio.
Employees will gain visibility into various types of submissions including Investigational New Drugs and New Drug Applications across major brands like Sensodyne and Panadol.
Matching Summary
This role supports process improvements and ensures compliance within the electronic data management system for a world-leading consumer healthcare company.
Salary
Hourly: $24.50; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
FDA submission documentation review
Electronic Data Management System maintenance
Full-time on-site work in New Jersey
Microsoft Excel and Word proficiency
Nice-to-have
Experience with eDMS systems
Knowledge of eCTD structure
Ability to identify regulatory trends
Key Requirements
Enrolled in Science, Biology, or Pharmacy degree program
Graduation between December 2026 and May 2028
Eligible to work in the US without future sponsorship
Available to start July 1, 2026
Minimum cumulative GPA of 3.0 preferred
Work Rights
Must be eligible to work in the US at time of employment